Investigation of somatic NKX2-5, GATA4 and HAND1 mutations in patients with tetralogy of Fallot
References (29)
- et al.
The incidence of congenital heart disease
J Am Coll Cardiol
(2002) - et al.
Novel NKX2-5 mutations in diseased heart tissues of patients with cardiac malformations
Am J Pathol
(2004) - et al.
Tetralogy of Fallot
Lancet
(2009) - et al.
GATA4 mutations in 486 Chinese patients with congenital heart disease
Eur J Med Genet
(2008) - et al.
Bicuspid aortic valve and ascending aortic aneurysm are not associated with germline or somatic homeobox NKX2-5 gene polymorphism in 19 patients
J Thorac Cardiovasc Surg
(2006) - et al.
Quantitation ofDNA extracted after micropreparation of cells from frozen and formalin-fixed tissue sections
Am J Pathol
(2000) - et al.
Effect of fixatives and tissue processing on the content and integrity of nucleic acids
Am J Pathol
(2002) - et al.
A high frequency of sequence alterations is due to formalin fixation of archival specimens
Am J Pathol
(1999) - et al.
Importance of gene-environment interac-tions in the etiology of selected birth defects
Clin Genet
(2009) - et al.
Genetic factors in non-syndromic congenital heart malformations
Clin Genet
(2010)
Congenital heart disease caused by mutations in the transcription factor NKX2-5
Science
(1998)
Somatic NKX2-5 mutations as a novel mechanism of disease in complex congenital heart disease
J Med Genet
(2004)
TBX5 mutations in non-Holt-Oram syn-drome (HOS) malformed hearts
Hum Mutat
(2004)
GATA4 zinc finger mutations as a molecular rationale for septation defects of the human heart
J Med Genet
(2005)
Cited by (0)
Copyright © 2011 Royal College of Pathologists of Australasia. Published by Elsevier B.V. All rights reserved.